Jensen Jeffrey T, Addis Ilana B, Hennebold Jon D, Bogan Randy L
Division of Reproductive and Developmental Science, Oregon National Primate Research Center, Beaverton, Oregon 97006.
Department of Obstetrics and Gynecology, Oregon Health & Science University, Portland, Oregon 97239.
J Clin Endocrinol Metab. 2017 Sep 1;102(9):3138-3145. doi: 10.1210/jc.2016-3456.
The premenopausal circulating lipid profile may be linked to the hormonal profile and ovarian lipid metabolism.
Assess how estradiol, progesterone, and ovarian lipid metabolism contributes to the premenopausal lipid profile; and evaluate the acute effects of a common hormonal oral contraceptive (OC) on circulating lipids.
Experimental crossover with repeated measures.
Academic hospitals.
Eight healthy, regularly menstruating women.
Participants underwent periodic serum sampling during a normal menstrual cycle; a standard 21-day, monophasic combined hormonal OC cycle (30 µg of ethinyl estradiol and 150 µg of levonorgestrel per day); menopause simulated by leuprolide acetate (22.5-mg depot); and an artificial menstrual cycle achieved via transdermal estradiol (50 to 300 µg/d) and vaginal micronized progesterone (100 to 300 mg/d).
Primary outcomes included evaluation of total cholesterol, high-density lipoprotein (HDL) cholesterol, low-density lipoprotein cholesterol, triglycerides, and the total cholesterol to HDL cholesterol ratio. To estimate the effect of estradiol, progesterone, and ovarian lipid metabolism, all specimens except those from the OC cycle were analyzed. Subgroup analysis was conducted on the follicular and luteal phases. In a separate analysis, the effect of the OC was evaluated relative to the normal menstrual cycle.
Estradiol was significantly associated with increased levels of HDL cholesterol throughout the menstrual cycle and in the follicular phase. Ovarian effects were associated with reduced lipid levels, especially during the luteal phase. The OC was associated with an increased total cholesterol to HDL cholesterol ratio and triglycerides.
Previously unappreciated factors including ovarian lipid metabolism may contribute to the premenopausal lipid profile.
绝经前的循环脂质谱可能与激素谱及卵巢脂质代谢有关。
评估雌二醇、孕酮和卵巢脂质代谢如何影响绝经前脂质谱;并评估一种常见的激素口服避孕药(OC)对循环脂质的急性影响。
重复测量的实验性交叉研究。
学术医院。
8名健康、月经周期规律的女性。
参与者在正常月经周期中进行定期血清采样;进行一个标准的21天单相联合激素OC周期(每天30μg炔雌醇和150μg左炔诺孕酮);用醋酸亮丙瑞林(22.5mg长效制剂)模拟绝经;通过经皮雌二醇(50至300μg/天)和阴道微粒化孕酮(100至300mg/天)实现人工月经周期。
主要结局包括评估总胆固醇、高密度脂蛋白(HDL)胆固醇、低密度脂蛋白胆固醇、甘油三酯以及总胆固醇与HDL胆固醇之比。为评估雌二醇、孕酮和卵巢脂质代谢的影响,对除OC周期样本外的所有样本进行分析。在卵泡期和黄体期进行亚组分析。在另一项分析中,相对于正常月经周期评估OC的影响。
在整个月经周期及卵泡期,雌二醇与HDL胆固醇水平升高显著相关。卵巢的影响与脂质水平降低有关,尤其是在黄体期。OC与总胆固醇与HDL胆固醇之比及甘油三酯升高有关。
包括卵巢脂质代谢在内的先前未被重视的因素可能影响绝经前脂质谱。